CLN5 rabbit pAb

Ref. EK-ES4682

Informations sur le produit

• Nom: CLN5 rabbit pAb
• Synonymes: CLN5; Ceroid-lipofuscinosis neuronal protein 5; Protein CLN5

Description

ceroid-lipofuscinosis, neuronal 5(CLN5) Homo sapiens This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008],

• Marque: ELK Biotechnology